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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >LC-MSn and HR-MS characterization of secondary metabolites from Hypericum japonicum Thunb. ex Murray from Nepalese Himalayan region and assessment of cytotoxic effect and inhibition of NF-kappa B and AP-1 transcription factors in vitro
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LC-MSn and HR-MS characterization of secondary metabolites from Hypericum japonicum Thunb. ex Murray from Nepalese Himalayan region and assessment of cytotoxic effect and inhibition of NF-kappa B and AP-1 transcription factors in vitro

机译:来自Hypericum japonicum thunb的二次代谢物的LC-MSN和HR-MS表征。 来自Nepalese Himalayan地区的EX Murray和体外抑制NF-Kappa B和AP-1转录因子的评估

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Hypericum japonicum Thunb. ex Murray is traditionally used in Nepal to treat several diseases, among whom inflammation and acute pain. Although several secondary metabolites from the same Hypericum species have been already characterized and considered for their pharmacological use, an exhaustive phytochemical characterization of H. japonicum from Nepal is lacking, as well as the assessment of its potential pharmacological properties. Hence, the aims of this study were the characterization of a methanolic extract of H. japonicum (HJME) collected from the Northern region of Nepal by LC-MSn and UPLC-QTOF. The assessment of in vitro inhibition of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kappa B) and activator protein 1 (AP-1) transcription factors and HJME's cytotoxic effect on human cell lines was performed to evaluate the potential use of this herb as a source of anti-inflammatory and cytotoxic lead compounds. Fifty-seven phytoconstituents were identified, being mainly flavonoids, phloroglucinols, phenolic acids and xanthones. Although compounds characteristic of H. japonicum were detected (quercetin, quercetin-7-O-alpha-l-rhamnoside, quercitrin and hyperoside), several others are here reported for the first time in this species. The results from bioassays indicated that HJME could significantly reduce the viability of human THP-1 cells (IC50 = 5.4 +/- 1.1 mu g mL(-1)), showing the promising potential of HJME as anti-tumor agent. Furthermore, HJME significantly decreased the activation of both NF-kappa B and AP-1 at the concentration of 2 mu g mL(-1). Overall, these data suggest that H. japonicum from Nepal could be used as a source of potential natural anti-inflammatory and anti-tumor lead compounds. (C) 2019 Elsevier B.V. All rights reserved.
机译:Hypericum japonicum thunb。 Ex Murray传统上用于尼泊尔治疗几种疾病,其中炎症和急性疼痛。尽管已经表征了来自相同的金属物种的几种次级代谢物,并且考虑了它们的药理学用途,但缺乏来自尼泊尔的H.Paponicum的详尽植物化学表征,以及评估其潜在的药理学性质。因此,该研究的目的是由LC-MSN和UPLC-QTOF从尼泊尔北部地区收集的H.Paponicum(HJME)的甲醇提取物的表征。进行了对活化B细胞(NF-Kappa B)和活化剂蛋白1(AP-1)转录因子和HJME对人细胞系的细胞毒性作用的体外抑制的评估进行评估,评估潜在使用该草本植物作为抗炎和细胞毒性铅化合物的来源。鉴定了五十七种植物选,主要是黄酮类化合物,甘油糖醇,酚醛酸和X原蝶。虽然检测到H. japonicum的化合物特征(槲皮素,槲皮素,槲皮素-7-o-α-l- rhamnoside,Quercietrin和hyperoary),其中几种在本物种中首次报道。生物测定的结果表明,HJME可以显着降低人THP-1细胞的活力(IC50 = 5.4 +/-1.1μg(-1)),显示HJME作为抗肿瘤剂的有希望的电位。此外,HJME在2μgmm(-1)的浓度下显着降低了NF-κB和AP-1的活化。总体而言,这些数据表明,来自尼泊尔的H.Paponicum可以用作潜在的天然抗炎和抗肿瘤铅化合物的来源。 (c)2019 Elsevier B.v.保留所有权利。

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